A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1506



Internal ID15199383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41824733..41857173hg38UCSC Ensembl
Outerchr15:42116931..42149371hg19UCSC Ensembl
Outerchr15:39904223..39936663hg18UCSC Ensembl
Outerchr15:39904223..39936663hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386998
hg196998
hg186998
hg176998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6630
SamplesNA12156
Known GenesJMJD7, JMJD7-PLA2G4B, MAPKBP1, PLA2G4B, SPTBN5
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1506
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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